Safety and Efficacy of Proellex in Pre-menopausal Anemic Women With Symptomatic Uterine Fibroids
Public ClinicalTrials.gov record NCT00702702. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
A Multi-Center, Placebo Controlled, Safety and Efficacy Study of the Selective Progesterone Receptor Modulator Proellex® (CDB-4124) in Anemic, Pre-Menopausal Women With Symptomatic Uterine Fibroids Requiring Hysterectomy
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
Eligible female subjects will be randomly assigned to one of the three treatment groups. Subjects will receive 325 mg (65 mg elemental iron) iron supplements to be taken twice daily during study drug treatment. The study duration is approximately six months, which is comprised of a 4 - 6 week screening period, a three-month drug treatment period, and a one-month follow-up period.
Study identification
- NCT ID
- NCT00702702
- Recruitment status
- Terminated
- Study type
- Interventional
- Phase
- Phase 3
- Enrollment
- 56 participants
Conditions and interventions
Conditions
Eligibility (public fields only)
- Age range
- 18 Years to 45 Years
- Sex
- Female
- Healthy volunteers
- Healthy volunteers not accepted
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Jun 2008 (Type not available)
- Primary completion
- Aug 2009 (Actual)
- Completion
- Aug 2009 (Actual)
- Last update posted
- Aug 21, 2014
2008 – 2009
United States locations
- U.S. sites
- 30
- U.S. states
- 14
- U.S. cities
- 24
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Alabama Clinical Therapeutics | Birmingham | Alabama | 35235 | — |
| Women's Health Research | Phoenix | Arizona | 85015 | — |
| Advanced Clinical Research Institute | Anaheim | California | 92801 | — |
| Impact Clinical Trials | Los Angeles | California | 90057 | — |
| National Institute of Clinical Research | Los Angeles | California | 90057 | — |
| Downtown Women's Health Care | Denver | Colorado | 80218 | — |
| Visions Clinical Research | Boynton Beach | Florida | 33472 | — |
| OB-GYN Associates of Mid-Florida, P.A. | Leesburg | Florida | 34748 | — |
| Segal Institute for Clinical Research | Miami | Florida | 33161 | — |
| Insignia Clinical Research (Tampa Bay Women's Center) | Tampa | Florida | 33607 | — |
| Comprehensive Clinical Trials, LLC | West Palm Beach | Florida | 33409 | — |
| Phoenix Women's Center (eCast) | College Park | Georgia | 30349 | — |
| Clinical Trials Select (ecast) | Decatur | Georgia | 30030 | — |
| Dekalb Gynecology Associates/Legacy Obstetrics & Gynecology (eCast) | Decatur | Georgia | 30035 | — |
| Medical Network for Education and Research | Decatur | Georgia | 30333 | — |
| Smith & Hackney | Morrow | Georgia | 30260 | — |
| Bluegrass Clinical Research, Inc. | Louisville | Kentucky | 40291 | — |
| Clinical Trials Select (ecast) | Silver Spring | Maryland | 20903 | — |
| Phoenix OB-GYN Associates, LLC | Moorestown | New Jersey | 08057 | — |
| Central Brooklyn Medical Group (eCast) | Brooklyn | New York | 11205 | — |
| Rapid Medical Research, Inc.(Elite) | Cleveland | Ohio | 44122 | — |
| HWC Women's Research Center | Englewood | Ohio | 45322 | — |
| SC Clinical Research Center | Columbia | South Carolina | 29201 | — |
| Chattanooga Medical Research, LLC | Chattanooga | Tennessee | 37404 | — |
| Advanced Research Associates | Corpus Christi | Texas | 78414 | — |
| Advances in Health Inc. | Houston | Texas | 77030 | — |
| The Women's Hospital of Texas, Clinical Research Center | Houston | Texas | 77054 | — |
| Centex Research | Houston | Texas | 77079 | — |
| Institute for Women's Health | San Antonio | Texas | 78229 | — |
| Seven Oaks Women's Center | San Antonio | Texas | 78229 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT00702702, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Aug 21, 2014 · Synced Oct 21, 2026
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Open the official record
The complete public registry record, listed eligibility criteria, and available contact information for NCT00702702 live on ClinicalTrials.gov.